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Updated: Jun 14, 2025

Measurement of Chitinase Activity in Biological Samples
Published on: August 22, 2019
Chitinase-3-Like 1 Protein (CHI3L1) Levels in Patients With Cognitive Deficits and Movement Disorders: Comparison
R Novobilský1,2,3, P Bártová1,2, D Stejskal4,3
1Department of Neurology, University Hospital Ostrava, Ostrava, Czech Republic.
Serum Chitinase-3-like protein 1 (CHI3L1) can help assess cognitive decline severity in neurodegenerative diseases. This study established its reference interval and diagnostic accuracy, supporting its use as a biomarker.
Area of Science:
- Neurology
- Biochemistry
- Biomarker Discovery
Background:
- Chitinase-3-like protein 1 (CHI3L1) is a glycoprotein linked to neuroinflammation and tissue remodeling in neurological conditions.
- Its role as a biomarker in neurodegenerative diseases requires further validation.
Purpose of the Study:
- To establish the reference interval (RI) for serum CHI3L1 (S CHI3L1) in healthy individuals.
- To correlate S CHI3L1 levels with established biomarkers of neurodegenerative damage.
- To evaluate the diagnostic accuracy of S CHI3L1 for cognitive disorders.
Main Methods:
- Serum samples from 108 healthy volunteers were analyzed to determine the S CHI3L1 RI.
- ELISA assays were used to measure S CHI3L1, neurofilament light chain (NfL), beta-amyloid, tau protein, and alpha-synuclein in patients with cognitive disorders.
- Cognitive function was assessed using the Mini-Mental State Examination (MMSE).
Main Results:
- The RI for S CHI3L1 was determined to be 14.44–63.11 µg/L, with a cut-off value of 34.37 µg/L.
- S CHI3L1 demonstrated 81.4% sensitivity and 76.9% specificity in ROC analysis.
- Significant correlations were observed between S CHI3L1 and age, S CHI3L1 and S NfL, and S CHI3L1 levels varied significantly across diagnostic groups.
Conclusions:
- Serum CHI3L1 levels correlate with cognitive deficit severity as measured by the MMSE.
- S CHI3L1 can serve as a valuable supportive biomarker in the diagnosis and monitoring of neurodegenerative diseases.
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